FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term retinitis pigmentosa 98 ID (Ontology) DOID:0061109 (Human Disease)
Definition A retinitis pigmentosa characterized by onset of night blindness in early childhood, with gradual loss of peripheral vision and later of central vision that has_material_basis_in homozygous or compound heterozygous mutation in the TMEM216 gene on chromosome 11q12.
Also Known As "RP98"
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 Genes
 retinitis pigmentosa 98       2
 for disease ribbon | retinitis pigmentosa 98       2
 model of | retinitis pigmentosa 98       2
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease__
retinal degeneration             |
 |__retinitis pigmentosa_________|
                                 retinitis pigmentosa 98  2 rec.
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Is a autosomal recessive disease
retinitis pigmentosa
Part of
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Synonyms
  • "RP98" EXACT OMO:0003012
Secondary IDs
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MIM:620996